Entrada Therapeutics Announces Recipients of Fourth Annual DREAMS Grant Program
Entrada awards two $50,000 DREAMS grants to U.S. and Dutch non-profits targeting more equitable access to Duchenne care and support.
Rhea-AI Summary
Entrada Therapeutics (TRDA) named Parent Project Muscular Dystrophy and Duchenne Parent Project Netherlands as the 2026 recipients of its DREAMS Grant Program, which awards two $50,000 grants to non-profit projects addressing disparities in the Duchenne muscular dystrophy community.
PPMD will use its grant to apply findings from a national Care Landscape Assessment across its Certified Duchenne Care Center network, aiming to improve access to coordinated, multidisciplinary care, particularly for adults and people in rural U.S. communities. Funds will support adult care infrastructure, multilingual resources, provider education and community engagement.
Duchenne Parent Project Netherlands will expand its Duchenne Barrier Breaker early-intervention program, embedding personalized coaching into routine Duchenne care in the Netherlands to promote autonomy, self-confidence and social participation during the transition to adulthood. An independent, multi-country Grant Review Committee of clinicians, advocates and individuals living with Duchenne selected the recipients.
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Key Figures
- Grant awards
- Two $50,000 grants
- 2026 DREAMS Grant Program
Key Terms
duchenne muscular dystrophy medical
patient-reported outcomes database technical
AI-generated analysis. How Rhea-AI works. Not financial advice.
-- Announced following World Duchenne Awareness Day on September 7, grants are designed to support projects bridging healthcare disparities across the global Duchenne community --
BOSTON, Sept. 10, 2026 (GLOBE NEWSWIRE) -- Entrada Therapeutics, Inc. (Nasdaq: TRDA) today announced the recipients of its 2026 DREAMS Grant Program: a competitive annual program that awards two
Entrada DREAMS Grant Recipients
- Parent Project Muscular Dystrophy (PPMD) is a U.S.-based patient advocacy organization that for more than 30 years has worked to accelerate the development of therapies, strengthen standards of care and advance policies benefiting the Duchenne and Becker muscular dystrophy communities. PPMD also manages The Duchenne Registry, the world’s largest patient-reported outcomes database for Duchenne and Becker. Earlier in 2026, PPMD embarked on a national Care Landscape Assessment through its Certified Duchenne Care Center (CDCC) network to better understand how individuals living with Duchenne access coordinated, multidisciplinary care across the lifespan. The DREAMS Grant will enable PPMD to operationalize learnings from the assessment and take steps to improve outcomes and create scalable models for access to specialized Duchenne care for underserved communities, with a focus on adults and individuals living in rural communities. By investing in adult care infrastructure, multilingual resources, provider education and community engagement, this project will establish lasting resources that continue to improve equitable access over time.
- Duchenne Parent Project Netherlands is a parent-founded organization committed to improving the lives of people living with Duchenne muscular dystrophy. It supports and funds research into new treatments and a cure, while advocating for better care, support and quality of life. One of its actions is to mobilize scientists, doctors and companies to accelerate research for Duchenne. Funds from the 2026 DREAMS Grant will support further implementation of Duchenne Barrier Breaker (DBB), an innovative early-intervention program designed to promote autonomy, self-confidence and social participation as individuals living with Duchenne transition into adulthood. Knowing that social and environmental factors can influence one’s ability to navigate daily life, Duchenne Parent Project Netherlands will work to ensure equitable access to personalized coaching by embedding the DBB into routine Duchenne care in the Netherlands.
“Parent Project Muscular Dystrophy’s and Duchenne Parent Project Netherlands’ initiatives serve as true models of this year’s World Duchenne Awareness Day theme, ‘access changes lives.’ It’s a privilege to support the efforts of two leading organizations who are working to advance equitable access to specialized support for all individuals living with Duchenne. As this year’s recipients work to bridge healthcare disparities in the U.S. and the Netherlands, I believe the impact of these efforts will extend across borders and shape the delivery of Duchenne care on a global scale,” said Dipal Doshi, Chief Executive Officer at Entrada Therapeutics.
Entrada thanks the 2026 DREAMS Independent Grant Review Committee for their time and dedication to selecting projects with the greatest potential to translate funding into lasting impact. The committee intentionally reflects the diversity and unique perspectives of the global Duchenne community, with members representing three countries and bringing critical expertise as patient advocates, neuromuscular researchers, care specialists and individuals living with Duchenne themselves:
- Annemieke Aartsma-Rus, PhD, Professor of Translational Genetics, Leiden University Medical Center
- Yuva Gambhir, Student, University of Pennsylvania, living with Duchenne
- Enrico Iovene, Student, University of Rome, living with Duchenne
- Amaris Sánchez-Larragoity, PsyD, Psychologist
- Aravindhan Veerapandiyan, MD, (Dr. Panda), Associate Professor of Pediatrics, Division of Pediatric Neurology, University of Arkansas for Medical Sciences at Arkansas Children’s Hospital
"It has been a privilege to serve on the Entrada DREAMS Grant Review Committee for the past four years and to witness firsthand the strength and innovation of organizations working to transform the Duchenne community,” said Aravindhan Veerapandiyan, MD, Pediatric Neurologist at University of Arkansas for Medical Sciences at Arkansas Children’s Hospital. “The 2026 applicants demonstrated an extraordinary commitment to addressing the unmet needs of the Duchenne community and creating meaningful, lasting change. Parent Project Muscular Dystrophy and Duchenne Parent Project Netherlands are uniquely positioned to improve access to critical resources and care for individuals living with Duchenne that have historically been underserved. I am excited to see how these programs empower individuals and families and help to advance a more equitable future for everyone living with Duchenne.”
About the DREAMS Grant Program
Launched by Entrada in 2023, DREAMS is a competitive annual grant program that funds non-profit organizations' efforts to advance equity, inclusion and accessibility within the Duchenne muscular dystrophy community. The program supports projects focused on better identifying, understanding and reaching individuals with Duchenne who are currently underrepresented or underserved, with the goal of improving equitable access to care and health outcomes. For more information, please visit DREAMS Grant Program on our corporate website.
Patients and Their Care Partners
Patients and their care partners are a critical part of our community, and we are committed to keeping them informed and connected. To receive community updates in real time and read today’s update, please visit Community Updates on our corporate website.
About Entrada Therapeutics
Entrada Therapeutics is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of genetic medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary, versatile and modular approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. The Company’s lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1.
For more information about Entrada, please visit our website, www.entradatx.com, and follow us on LinkedIn.
Patient Advocacy Contact
Sarah Friedhoff
Head of Patient Advocacy
patientadvocacy@entradatx.com
Media Contact
Megan Prock McGrath
CTD Comms, LLC
megan@ctdcomms.com
Investor Contact
Doug Snow
Head of Investor Relations
dsnow@entradatx.com
FAQ
What is the purpose of Entrada’s DREAMS Grant Program?
The DREAMS Grant Program, launched in 2023, is a competitive annual initiative that funds non-profit organizations working to advance equity, inclusion and accessibility within the Duchenne muscular dystrophy community. It focuses on projects that better identify, understand and reach individuals with Duchenne who are underrepresented or underserved, with the goal of improving equitable access to care and health outcomes.
How are DREAMS Grant recipients selected each year?
An Independent Grant Review Committee composed of neuromuscular specialists, patient advocates, health equity advocates and individuals living with Duchenne reviews applications and selects one U.S.-based non-profit and one non-profit in the U.K. or EU. The committee members represent three countries and bring expertise as researchers, care specialists, psychologists, students living with Duchenne and patient advocates.
How will Parent Project Muscular Dystrophy use its 2026 DREAMS grant?
Parent Project Muscular Dystrophy plans to use the grant to operationalize learnings from its national Care Landscape Assessment conducted through the Certified Duchenne Care Center network. The project will work to improve access to specialized, coordinated Duchenne care for underserved U.S. communities, with a particular emphasis on adults and people in rural areas, supported through adult care infrastructure, multilingual resources, provider education and community engagement.
What will Duchenne Parent Project Netherlands do with its DREAMS funding?
Duchenne Parent Project Netherlands will use the 2026 DREAMS Grant to further implement its Duchenne Barrier Breaker early-intervention program. The organization plans to embed personalized coaching into routine Duchenne care in the Netherlands so that individuals transitioning into adulthood can gain autonomy, self-confidence and social participation, with attention to equitable access to these coaching resources.
Where can patients and caregivers find more information or updates from Entrada?
Patients and their care partners can receive real-time community updates and read this announcement by visiting the Community Updates section on Entrada Therapeutics’ corporate website. Additional information about the DREAMS Grant Program is available on the same site.